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  • MD Atlas
  • Documents

Chetan Meditech Pvt. Ltd.

Certificate 2024-MDR/TD-032

Rev. 00Issued
Valid until
Jul 1, 2029

Certificate 2024-MDR/TD-032 is a valid Technical documentation issued to Chetan Meditech Pvt. Ltd. and registered in EUDAMED. Valid until July 1, 2029. View the full certificate record on MD Atlas.

Overview

Certificate number
2024-MDR/TD-032
Certificate type
Technical documentation
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
22652024-MDR/TD-03200

Validity

Issued
Jul 1, 2024
Valid from
Jul 1, 2024
Valid until
Jul 1, 2029

Notified body

Notified body
3EC International a.s.
Notified body SRN
2265
Notified body country
Slovakia

Characteristics

Sterile
—
Human tissues
—
Animal tissues
—
In vitro diagnostics
—
Initial registration
Yes
New device
No
Discard allowed
No
SSCP enabled
Yes
Mechanism of scrutiny
No
Intended medical purpose
—
SPP applicable
—
Conditions applicable
No
MOS outside EUDAMED
—
QMS/MOS type
Others

History

No status changes or preceding certificates are recorded.

Scope coverage

Unspecified1

1 scope

  • BIOTEK, MICRO-VIM, MINI-VIM, SUPER-VIM, SUPER-VIM III, SUPER-VIM L, MICRO-VIM PK, MINI-VIM PK, MINI-VIM II PK, VIMFIX-PK, VIMFIX-PK III, VIMFIX-LRP, VIMFIX- LRT, VIMFIX-BT, FIBERKNOT
    89042103cmplimp002X9

Documents

LanguagesEN

Manufacturer

Manufacturer
Chetan Meditech Pvt. Ltd.
Manufacturer SRN
IN-MF-000013541
Manufacturer country
India

Covered devices

  • BIOTEK, MICRO-VIM, MINI-VIM, SUPER-VIM, SUPER-VIM III, SUPER-VIM L, MICRO-VIM PK, MINI-VIM PK, MINI-VIM II PK, VIMFIX-PK, VIMFIX-PK III, VIMFIX-LRP, VIMFIX- LRT, VIMFIX-BT, FIBERKNOTClass IIb
    89042103cmplimp002X9

Linked SSCPs

  • SSCP SSCP/02